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Updated: May 12, 2026

Diagnosis of Neoplasia in Barrett’s Esophagus using Vital-dye Enhanced Fluorescence Imaging
Published on: May 11, 2014
Biomarker Use in Barrett's Esophagus Surveillance
Annesha Chatterjee1, Julian A Abrams2, Matthew D Stachler1
1Department of Pathology and Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.
None:
Barrett's esophagus (BE) is the established precursor to esophageal adenocarcinoma; however, the overwhelming majority of patients with BE never progress to cancer. Therefore, there is a clinical need to identify the patients with BE who are at high risk of progression from the patients with BE who will not progress. Histologic dysplasia has served as the marker of progression risk on which clinical decisions are made. However, dysplasia assessment in practice has been hindered by high interobserver variability. As such, many studies to develop validated biomarkers that either assist in dysplasia assessment or independently serve as predictors of progression risk have been performed. In this review, we will summarize some of these studies, primarily focused on p53, abnormal genomic content, and methylated DNA markers, which have shown promise for their ability to identify patients at increased risk of progressing to more advanced disease.
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